Review identifies CD248 as a promising therapeutic target for sarcomas and fibrotic diseases, suggesting implications for cancer treatment.
Since its discovery more than 30 years ago, our understanding of the function of CD248 (also known as endosialin or TEM1) as a therapeutic target has evolved, and CD248 is now recognized as a potentially valuable target for therapeutics directed toward sarcomas and fibrotic diseases. The current study reviews the literature related to CD248 and examines CD248 expression across various models including patient-derived xenografts, patient-derived cell lines (pdmr.cancer.gov/), and large cell line collections, including the Cell Line Encyclopedia (CCLE) and the GDSC-MGH-Sanger. CD248 is highly and selectively expressed by sarcomas and by pericytes in tumor vasculature and wound-healing vasculature. It is a component of a multi-protein complex which connects various cell types into tissue structure. Multiple therapeutic approaches are being investigated to take advantage of CD248 in the treatment of sarcomas and fibrotic diseases. Endosialin/CD248/TEM1 is a promising biological target that remains poorly explored in cancer therapy. Importantly, CD248 is overexpressed in several human solid tumors and absent in most normal adult tissues, making it a suitable and potentially safe target for radioimmunotherapy, particularly in Ewing’s sarcoma xenograft models.
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Teicher et al. (2026) studied this question.
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